Evolution of Natural Product Scaffolds by Acyl- and Arylnitroso Hetero-Diels−Alder Reactions: New Chemistry on Piperine-Reference-Cited by-同舟云学术

Evolution of Natural Product Scaffolds by Acyl- and Arylnitroso Hetero-Diels−Alder Reactions: New Chemistry on Piperine

Published:2008-05-20 Issue:12 Volume:73 Page:4559-4567
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Krchňák Viktor¹,Waring Katherine R.¹,Noll Bruce C.¹,Moellmann Ute¹,Dahse Hans-Martin¹,Miller Marvin J.¹

Affiliation:

1. Department of Chemistry and Biochemistry, 251 Nieuwland Science Hall, University of Notre Dame, Notre Dame, Indiana 46556, and Leibniz Institute for Natural Product Research and Infection Biology – Hans Knoell Institute, Beutenbergstrasse 11a, 07745 Jena, Germany

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo8004827

Reference24 articles.

1. Solid-Supported Nitroso Hetero Diels–Alder Reactions. 1. Acylnitroso Dienophiles: Scope and Limitations

2. Solid-Supported Nitroso Hetero Diels–Alder Reactions. 2. Arylnitroso Dienophiles: Scope and Limitations

3. Iminonitroso Diels−Alder Reactions for Efficient Derivatization and Functionalization of Complex Diene-Containing Natural Products

4. Formation and dienophilic reactions of transient C-nitrosocarbonyl compounds

5. Graziani, E. I.; Pong, K.; Skotnicki, J.Rapamycin analogues and the uses thereof in the treatment of neurological, proliferative, and inflammatory disorders. U.S. Pat. Appl. Publ. 2006135549, 2006.

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